Cas 1367192-03-7,O-(2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl) stearyl glycyrrhetinate

1367192-03-7

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Basic information

Product Name: O-(2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl) stearyl glycyrrhetinate
Synonyms: O-(2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl) stearyl glycyrrhetinate
CAS NO:1367192-03-7
Molecular Formula:
Molecular Weight: 1197.73
EINECS: N/A
Product Categories: N/A
Mol File: 1367192-03-7.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: O-(2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl) stearyl glycyrrhetinate(CAS DataBase Reference)
NIST Chemistry Reference: O-(2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl) stearyl glycyrrhetinate(1367192-03-7)
EPA Substance Registry System: O-(2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl) stearyl glycyrrhetinate(1367192-03-7)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1367192-03-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1367192-03-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,7,1,9 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1367192-03:
(9*1)+(8*3)+(7*6)+(6*7)+(5*1)+(4*9)+(3*2)+(2*0)+(1*3)=167
167 % 10 = 7
So 1367192-03-7 is a valid CAS Registry Number.

1367192-03-7Upstream product

13832-70-7 glycyrrhetinyl stearate

1367192-03-7Downstream Products

1367192-03-7Relevant articles and documents

Direct O-glycosidation of resin bound thioglycosides

Nguyen, Son Hong,Trotta, Adam H.,Cao, John,Straub, Timothy J.,Bennett, Clay S.

supporting information; experimental part, p. 2373 - 2376 (2012/04/11)

The application of the safety-catch linker concept to solid-phase glycoconjugate synthesis is described. The process allows for direct conjugation of resin bound glycans to complex aglycones during cleavage. Large excesses of either coupling partner are not required, and even very hindered alcohols serve as acceptors in the reaction. The Royal Society of Chemistry 2012.

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